RecallHawk
Class I Recall

Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC: 0718

Vietti Acquisitions, LLC

Summary

The FDA issued a Class I for Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in by Vietti Acquisitions, LLC. Reason: Undeclared allergen (soy) due to mislabeling. Product is labeled as Brown Sugar Molasses Baked Beans, but contains Beef and BBQ Baked Beans. The Bee.

Details

Source

Food Recall

External ID

F-0806-2025

Action Date

2025-05-28

Status

Terminated

Category

food

Product Description

Yellowstone Brown Sugar Molasses Baked Beans, NET WT. 15 OZ (425g), packaged in cans, packed 12 cans per case. UPC: 071846187071; Packaged by: Vietti Foods Inc. Nashville, TN 37203

Lot/Code Info: Lot code: Best if Used By Feb 17, 2028 Code on can: 0652642B172580002 Case label: 12/15oz Yellowstone Beef and Baked Beans BBQ 80-002 B1725

Quantity Affected: 4,661 cases

Reason for Recall

Undeclared allergen (soy) due to mislabeling. Product is labeled as Brown Sugar Molasses Baked Beans, but contains Beef and BBQ Baked Beans. The Beef and BBQ Baked Beans contain soy, which is not declared on the label.

Distribution

Distributed through retailers in: AZ, CO, DE, FL, GA, IA, IL, KS, KY, LA, MI, MO, MS, NC, NH, NY, OH, OR, PA, TN, TX, UT, and VA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-02

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Vietti Acquisitions, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vietti Acquisitions, LLC have FDA actions?

This is the only FDA action we have on record for Vietti Acquisitions, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0806-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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